Canonical Allele Identifier: CA2450716895

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108680878T= , CM000685.2:g.108680878T=	GRCh38
NC_000023.10:g.107924108T= , CM000685.1:g.107924108T=	GRCh37
NC_000023.9:g.107810764T=	NCBI36
NG_011977.1:g.245955T=
NG_011977.2:g.245955T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4016-7T= MANE Select	ENSP00000331902.7:n.4016-7T=
ENST00000361603.7:c.3998-7T=	ENSP00000354505.2:n.3998-7T=
ENST00000510690.2:n.510-7T=
ENST00000328300.10:c.4016-7T=	ENSP00000331902.6:n.4016-7T=
ENST00000361603.6:c.3998-7T=	ENSP00000354505.2:n.3998-7T=
ENST00000489230.1:n.419-7T=
NM_000495.4:c.3998-7T=	NP_000486.1:n.3998-7T=
NM_033380.2:c.4016-7T=	NP_203699.1:n.4016-7T=
XM_005262070.2:c.4007-7T=	XP_005262127.1:n.4007-7T=
XM_006724616.2:c.4016-7T=	XP_006724679.1:n.4016-7T=
XM_011530849.1:c.3692-7T=	XP_011529151.1:n.3692-7T=
XM_011530851.1:c.1589-7T=	XP_011529153.1:n.1589-7T=
XM_011530849.2:c.4031-7T=	XP_011529151.2:n.4031-7T=
XM_017029259.2:c.4022-7T=	XP_016884748.1:n.4022-7T=
XM_017029260.1:c.4013-7T=	XP_016884749.1:n.4013-7T=
XM_017029263.2:c.2351-7T=	XP_016884752.1:n.2351-7T=
NM_000495.5:c.3998-7T=	NP_000486.1:n.3998-7T=
NM_033380.3:c.4016-7T= MANE Select	NP_203699.1:n.4016-7T=